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2-Bromopropane → 4-Bromo-1-isopropyl-1H-pyrazole

HRID 64057
ノート
印刷プレビュー

反応式

HRID 64057 の反応式
[Br:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1.C([O-])([O-])=O.[K+].[K+].Br[CH:14]([CH3:16])[CH3:15]>CN(C=O)C>[Br:1][C:2]1[CH:3]=[N:4][N:5]([CH:14]([CH3:16])[CH3:15])[CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 63582-BromopropaneHCID 11430Potassium CarbonateHCID 163754-Bromopyrazole

生成物 1

HCID 223292004-Bromo-1-isopropyl-1H-pyrazole収率 89%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 4-bromo-1H-pyrazole (5 g, 34 mmol) in DMF (70 ml) were added K2CO3 (11.83 g, 85.6 mmol, 2.5 eq.) and 2-bromopropane (6.3 g, 51.36 mmol, 1.5 eq.) and the mixture was stirred at RT for 12 h. The mixture was quenched and extracted as in Intermediate Example 5(a). The solvent was distilled off and the crude residue was purified by column chromatography (60-120 silica gel, 20% ethyl acetate in hexane) to afford the product in 89% yield (5.8 g). 1H NMR (300 MHz, DMSO-d6): δ 8.01 (s, 1H), 7.50 (s, 1H), 4.49-4.43 (m, 1H), 1.38 (d, 6H).

後処理

  1. customThe mixture was quenched
  2. extractionextracted as in Intermediate Example 5(a)
  3. distillationThe solvent was distilled off
  4. customthe crude residue was purified by column chromatography (60-120 silica gel, 20% ethyl acetate in hexane)
  5. customto afford the product in 89% yield (5.8 g)

出典と根拠

ORDレコード
ord-27cb84df084c4cb9be2332bc6cd068a1
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447091B2

反応ノート

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